Phase 2 Study of BA058 (Abaloparatide) Transdermal Delivery in Postmenopausal Women With Osteoporosis

• Status: Completed
• Trial end date: 2013-08-02
• Target enrollment: 0
• Participant gender: Female

Summary

To determine the clinical safety and efficacy of abaloparatide transdermal in otherwise healthy postmenopausal women with osteoporosis as assessed by changes in bone mineral density (BMD) and serum markers of bone metabolism when compared to transdermal placebo and abaloparatide injection for 6 months of treatment.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Radius Health, Inc.
• Collaborator: Nordic Bioscience A/S
• Treatments: Abaloparatide; Parathyroid Hormone-Related Protein

Criteria

Inclusion Criteria:

• Postmenopausal woman, less than 85 years old.

• BMD T-score ≤-2.5 of spine or hip (femoral neck) or ≤-2.0 with previous fracture (within 5 years).

• Normal physical exam, vital signs, electrocardiogram (ECG), and medical history.

• Laboratory tests within the normal range, including serum calcium, Vitamin D, parathyroid hormone (PTH) (1-84), serum phosphorus, and alkaline phosphatase.

Exclusion Criteria:

• BMD T-score ≤-5.0 at the lumbar spine or hip.

• History of bone disorders (for example, Paget's disease) other than postmenopausal osteoporosis.

• Significantly impaired renal function.

• History of any cancer.